Study of addition of opioid to local anaesthetic in regional anaesthesia in cesarean sectio
Phase 4
Completed
- Conditions
- Health Condition 1: null- Quality of anaesthesia and duration of postoperative analgesia in patient undergoing elective cesarean section under epidural anaesthesia
- Registration Number
- CTRI/2014/06/004698
- Lead Sponsor
- Government Medical College Nagpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 64
Inclusion Criteria
Full term patients undergoing elective cesarean section.
Exclusion Criteria
Foetal distress, moderate to severe PIH, Patients refusal, conversion to general anaesthsia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is intraoperative VAS score.Timepoint: Immediately after completion of surgery VAS score will be assessed.
- Secondary Outcome Measures
Name Time Method The secondary outcome were the fentanyl related side effects, intraoperative haemodynamic changes, onset of analgesia, volume of drug required to achieve T6 level, quality and duration of motor block and adverse events in newborn.Timepoint: till first analgesic demand